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A marker gene-based method for identifying the cell-type of origin from single-cell RNA sequencing data
Single-cell RNA sequencing (scRNA-seq) experiments provide opportunities to peer into complex tissues at single-cell resolution. However, insightful biological interpretation of scRNA-seq data relies upon precise identification of cell types. The ability to identify the origin of a cell quickly and...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10326446/ https://www.ncbi.nlm.nih.gov/pubmed/37424758 http://dx.doi.org/10.1016/j.mex.2023.102196 |
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author | Nouri, Nima Gaglia, Giorgio Kurlovs, Andre H. de Rinaldis, Emanuele Savova, Virginia |
author_facet | Nouri, Nima Gaglia, Giorgio Kurlovs, Andre H. de Rinaldis, Emanuele Savova, Virginia |
author_sort | Nouri, Nima |
collection | PubMed |
description | Single-cell RNA sequencing (scRNA-seq) experiments provide opportunities to peer into complex tissues at single-cell resolution. However, insightful biological interpretation of scRNA-seq data relies upon precise identification of cell types. The ability to identify the origin of a cell quickly and accurately will greatly improve downstream analyses. We present Sargent, a transformation-free, cluster-free, single-cell annotation algorithm for rapidly identifying the cell types of origin based on cell type-specific markers. We demonstrate Sargent's high accuracy by annotating simulated datasets. Further, we compare Sargent performance against expert-annotated scRNA-seq data from human organs including PBMC, heart, kidney, and lung. We demonstrate that Sargent retains both the flexibility and biological interpretability of cluster-based manual annotation. Additionally, the automation eliminates the labor intensive and potentially biased user annotation, producing robust, reproducible, and scalable outputs. • Sargent is a transformation-free, cluster-free, single-cell annotation algorithm for rapidly identifying the cell types of origin based on cell type-specific markers. • Sargent retains both the flexibility and biological interpretability of cluster-based manual annotation. • Automation eliminates the labor intensive and potentially biased user annotation, producing robust, reproducible, and scalable outputs. |
format | Online Article Text |
id | pubmed-10326446 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-103264462023-07-08 A marker gene-based method for identifying the cell-type of origin from single-cell RNA sequencing data Nouri, Nima Gaglia, Giorgio Kurlovs, Andre H. de Rinaldis, Emanuele Savova, Virginia MethodsX Bioinformatics Single-cell RNA sequencing (scRNA-seq) experiments provide opportunities to peer into complex tissues at single-cell resolution. However, insightful biological interpretation of scRNA-seq data relies upon precise identification of cell types. The ability to identify the origin of a cell quickly and accurately will greatly improve downstream analyses. We present Sargent, a transformation-free, cluster-free, single-cell annotation algorithm for rapidly identifying the cell types of origin based on cell type-specific markers. We demonstrate Sargent's high accuracy by annotating simulated datasets. Further, we compare Sargent performance against expert-annotated scRNA-seq data from human organs including PBMC, heart, kidney, and lung. We demonstrate that Sargent retains both the flexibility and biological interpretability of cluster-based manual annotation. Additionally, the automation eliminates the labor intensive and potentially biased user annotation, producing robust, reproducible, and scalable outputs. • Sargent is a transformation-free, cluster-free, single-cell annotation algorithm for rapidly identifying the cell types of origin based on cell type-specific markers. • Sargent retains both the flexibility and biological interpretability of cluster-based manual annotation. • Automation eliminates the labor intensive and potentially biased user annotation, producing robust, reproducible, and scalable outputs. Elsevier 2023-04-25 /pmc/articles/PMC10326446/ /pubmed/37424758 http://dx.doi.org/10.1016/j.mex.2023.102196 Text en © 2023 Published by Elsevier B.V. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Bioinformatics Nouri, Nima Gaglia, Giorgio Kurlovs, Andre H. de Rinaldis, Emanuele Savova, Virginia A marker gene-based method for identifying the cell-type of origin from single-cell RNA sequencing data |
title | A marker gene-based method for identifying the cell-type of origin from single-cell RNA sequencing data |
title_full | A marker gene-based method for identifying the cell-type of origin from single-cell RNA sequencing data |
title_fullStr | A marker gene-based method for identifying the cell-type of origin from single-cell RNA sequencing data |
title_full_unstemmed | A marker gene-based method for identifying the cell-type of origin from single-cell RNA sequencing data |
title_short | A marker gene-based method for identifying the cell-type of origin from single-cell RNA sequencing data |
title_sort | marker gene-based method for identifying the cell-type of origin from single-cell rna sequencing data |
topic | Bioinformatics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10326446/ https://www.ncbi.nlm.nih.gov/pubmed/37424758 http://dx.doi.org/10.1016/j.mex.2023.102196 |
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